Showing results (751-760 of 1,845) with videos related to

Sort By:
Pageof 185
Ophthalmic Genetics|December 11, 2020
Novel FZD4 and LRP5 mutations in a small cohort of patients with familial exudative vitreoretinopathy (FEVR)William Carrera, Caleb Ng, Caroline Desler, et al.
Ophthalmic Genetics|December 17, 2021
A homozygous in-frame duplication within the LRRCT consensus sequence of CFAP410 causes cone-rod dystrophy, macular staphyloma and short statureNing Chiu, Winston Lee, Pei-Kang Liu, et al.
Ophthalmic Genetics|January 11, 2022
Penetrance of MYOC gene mutation in primary open-angle glaucoma: A systematic review and meta-analysisJuan-Juan Xie, Guo-Wei Zhang, Hai-Yue Cui, et al.
Ophthalmic Genetics|January 21, 2022
Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophyAndrew J Catomeris, Brian G Ballios, Riccardo Sangermano, et al.
Ophthalmic Genetics|November 5, 2021
A novel stop codon mutation of TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathyGang Zou, Rui Qi, Meijiao Ma, et al.
Ophthalmic Genetics|December 10, 2021
Macular atrophy in JAG1-related Alagille syndrome: a case seriesManuel Paez-Escamilla, Hannah L Scanga, Alkiviades Liasis, et al.
Ophthalmic Genetics|December 30, 2021
An extended phenotype of RP1L1 maculopathy - case reportGeorge J Manayath, Mayur Rokdey, Shishir Verghese, et al.
Ophthalmic Genetics|December 27, 2021
Photoaversion in inherited retinal diseases: clinical phenotypes, biological basis, and qualitative and quantitative assessmentSerena Zaman, Thomas Kane, Mohamed Katta, et al.
Ophthalmic Genetics|December 27, 2021
OTX2 mutation associated with severe myopia in a Canadian familySnow Wangding, Samantha Colaiacovo, Inas Makar, et al.
Ophthalmic Genetics|December 8, 2021
Cone pathway dysfunction in Jalili syndrome due to a novel familial variant of CNNM4 revealed by pupillometry and electrophysiologic investigationsRobert A Hyde, Evelina Kratunova, Jason C Park, et al.
Pageof 185